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检索条件"作者=Maryam Erfanian Omidvar"
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Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndrome
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Genes & Diseases 2020年 第4期7卷 614-619页
作者: Hamid Ghaedi Samira Molaei Ramsheh maryam erfanian omidvar Afsaneh Labbaf Elham Alehabib Sanaz Akbari Fatemeh Pourfatemi Hossein Darvish Department of Medical Genetics School of MedicineShahid Beheshti University of Medical SciencesTehranIran Department of Medical Laboratory Technology School of Allied Medical SciencesShahid Beheshti University of Medical SciencesTehranIran Student Research Committee Department of Medical GeneticsSchool of MedicineShahid Beheshti University of Medical SciencesTehranIran Nourdanesh Institute MeymehIsfahanIran Deputy for Prevention Affairs of State Welfare Organization of Mazandaran SariIran Cancer Research Center Semnan University of Medical SciencesSemnanIran Department of Medical Genetics School of MedicineSemnan University of Medical SciencesSemnanIran
Hereditary nonpolyposis colorectal cancer or Lynch syndrome is autosomal dominant cancer predisposition syndrome characterized by early onset of colorectal cancer and neoplasia in other *** condition typically caused ... 详细信息
来源: 维普期刊数据库 维普期刊数据库 评论
Complementary Inequalities to Improved AM-GM Inequality
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Acta Mathematica Sinica,English Series 2017年 第12期33卷 1609-1616页
作者: Hamid Reza MORADI Mohsen erfanian omidvar Department of Mathematics Mashhad Branch Islamic Azad University Mashhad Iran
Following an idea of Lin, we prove that if A and B are two positive operators such that 0 〈 mI 〈 A 〈 m'I ≤ M'I ≤B 〈 MI, then Ф^2(A+B/2)≤K^2(h)/(1+(logM'/m')^2/8)^2Ф^2(A#B),and Ф^2(A+B/2)≤... 详细信息
来源: 维普期刊数据库 维普期刊数据库 同方期刊数据库 同方期刊数据库 评论